Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name Nebulizer (Direct Patient Interface)
510(k) Number K954327
Device Name MEDOX CHAMPION COMPACT NEBULIZER
Applicant
Medox Corp.
1400 Village Way
Santa Ana,  CA  92705
Applicant Contact EDWARD J BUZBY
Correspondent
Medox Corp.
1400 Village Way
Santa Ana,  CA  92705
Correspondent Contact EDWARD J BUZBY
Regulation Number868.5630
Classification Product Code
CAF  
Date Received09/15/1995
Decision Date 12/19/1995
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-